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Clinical Data Manager Jobs in Magnolia, MS (NOW HIRING)

Amaris Consulting

Clinical Research Coordinator

Mccomb, MS · On-site

$21 - $27.75/hr

We are looking for an Clinical Research Coordinator to support the day-to-day management and ... Experience in subject enrollment management, source documentation, data entry, adverse event ...

IQVIA

Field Nurse Educator

Mccomb, MS

$95K - $105K/yr

... manage their disease state and resources associated with their prescribed medication. Nurse ... Knowledge of clinical data and pharmacology * Valid driver's license * Ambassador must live in the ...

IQVIA

Field Nurse Educator - Hattiesburg, MS

Mccomb, MS · On-site

$95K - $105K/yr

... manage their disease state and resources associated with their prescribed medication. Nurse ... Knowledge of clinical data and pharmacology * Valid driver's license * Ambassador must live in the ...

IQVIA

Field Nurse Educator - Hattiesburg, MS

Mccomb, MS · On-site

$95K - $105K/yr

... manage their disease state and resources associated with their prescribed medication. Nurse ... Knowledge of clinical data and pharmacology * Valid driver's license * Ambassador must live in the ...

Forrest General Hospital

RN- Tylertown

Tylertown, MS · On-site

... Clinical Manager. The position requires that the individual be clinically competent and ... data reflective of the patient's status and interprets the appropriate information needed to ...

Forrest General Hospital

RN- Tylertown

Tylertown, MS · On-site

... Clinical Manager. The position requires that the individual be clinically competent and ... data reflective of the patient's status and interprets the appropriate information needed to ...

Forrest General Hospital

RN- Tylertown

Tylertown, MS · On-site

... Clinical Manager. The position requires that the individual be clinically competent and ... data reflective of the patient's status and interprets the appropriate information needed to ...

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Clinical Data Manager information

See Magnolia, MS salary details

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How much do clinical data manager jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical data manager in Magnolia, MS is $50.06, according to ZipRecruiter salary data. Most workers in this role earn between $39.57 and $59.57 per hour, depending on experience, location, and employer.

What does a clinical data manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

What does a clinical data manager do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

What are the key skills and qualifications needed to thrive as a clinical data manager?

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What are some common challenges clinical data managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

How much do clinical data managers make in the US?

Clinical data managers in the US typically earn between $70,000 and $110,000 annually, with salaries varying based on experience, education, and location. Entry-level positions may start around $60,000, while experienced professionals with specialized skills can earn over $120,000. Certifications in data management and proficiency with electronic data capture systems can also influence salary levels.
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What cities near Magnolia, MS are hiring for Clinical Data Manager jobs?

Cities near Magnolia, MS with the most Clinical Data Manager job openings:

Clinical Data Manager jobs near you
Infographic showing various Clinical Data Manager job openings in Magnolia, MS as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $104,127 per year, or $50.1 per hour.

Clinical Research Coordinator

Amaris Consulting

Mccomb, MS • On-site

$21 - $27.75/hr

Other

Posted 18 days ago

Job description

We are looking for an Clinical Research Coordinator to support the day-to-day management and execution of a clinical research study at an investigative site. You will serve as the primary liaison between investigators, sponsor, and site staff, ensuring the study is conducted in compliance with the protocol, Good Clinical Practice (GCP), regulatory requirements, and institutional policies.


Key Information:

  • Location: McComb, Mississippi, USA
  • Work Mode: hybrid
  • This is a part-time role requiring 2–3 days of work per week.
  • Length of contract: 4 months
  • Type of contract: C2C
  • Salary rate: 40-50 USD per hour


Key Tasks:

  • Coordinate patient enrollment activities
  • Collect, review, and maintain source documentation and study records
  • Enter study data into Electronic Data Capture (EDC) systems and resolve data queries
  • Maintain regulatory binders and essential study documentation
  • Prepare for and support sponsor monitoring visits, audits, and site inspections
  • Ensure participant safety, confidentiality, and protocol compliance throughout the study
  • Collaborate closely with investigators, radiology staff, and study teams to ensure protocol-required procedures are completed


Profile

Must-Haves:

  • Bachelor's degree in a related field
  • 5 years of Clinical Research Coordination experience
  • Experience conducting sponsored research studies
  • Strong understanding of ICH-GCP guidelines, FDA regulations, and IRB submissions
  • Experience with Electronic Data Capture (EDC) systems
  • Experience with Medidata Rave
  • Ability and willingness to travel on-site to support study activities
  • Strong organizational and communication skills
  • Experience in subject enrollment management, source documentation, data entry, adverse event reporting, site regulatory documentation, and query resolution

Nice-to-Haves:

  • Experience in an imaging environment (particularly CT) to support imaging-related study activities


Why choose us

  • An international community bringing together more than 110 different nationalities
  • An environment where trust is central: 70% of our leaders started their careers at the entry level
  • A strong training system with our internal Academy and more than 250 modules available
  • A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)


Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

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